HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486442Generated: October 31, 2026
2-(3,3-difluorocyclobutyl)ethan-1-ol → (3,3-Difluorocyclobutyl)acetic acid
https://huagongshe.com/reaction/1486442
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(3,3-difluorocyclobutyl)ethan-1-ol | HCID 72206954 | — |
| Reactant | Jones' reagent | HCID 131709961 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | (3,3-Difluorocyclobutyl)acetic acid | HCID 71743770 | 92% |
Reaction Steps
A solution of 2-(3,3-difluorocyclobutyl)ethanol (270 mg, 2.0 mmol, prepared as described in Bogen, S. et al., Bioorg. Med. Chem. Lett., 18:4219 (2008)) in acetone (5 mL) was treated with Jones reagent (2.7 mmol, 1 mL of 2.7 M solution) over a period of 30 minutes at room temperature. After 2 hours, additional Jones reagent (0.25 mL) was added. After 1 hour, the reaction mixture was filtered through CELITE®, and concentrated under reduced pressure. The reaction mixture was re-dissolved in ethyl acetate (10 mL), washed with water (2×20 mL), brine (20 mL), and then dried over MgSO4, The mixture was then filtered and concentrated to isolate Intermediate S-9A (275 mg, 92% yield) as a tan solid. 1H NMR (500 MHz, chloroform-d) δ 2.74-2.87 (2H, m), 2.57-2.62 (2H, m), 2.48-2.56 (1H, m, J=8.60, 4.30, 4.30, 1.94 Hz), 2.23-2.35 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09427442B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-1760725091bd406ba1f32acdd50979ce |
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| Source note | uspto-grants-2016_08 |
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